Ex Parte LINNENBACH et al - Page 11


                Appeal No.2001-1258                                                  Page 11                  
                Application No. 08/413,805                                                                    

                      “Obviousness does not require absolute predictability of success. . . .  For            
                obviousness under § 103, all that is required is a reasonable expectation of                  
                success.”  In re O’Farrell, 853 F.2d 894, 903-04, 7 USPQ2d 1673, 1681 (Fed.                   
                Cir. 1988).  In this case, we find that the references would have provided the                
                required reasonable expectation of success.                                                   
                      Finally, Appellants argue that the references do not suggest the                        
                composition of claim 4.  (See the Appeal Brief, pages 7-8).  Appellants argue that            
                “Szala and Bumol teach the use of antibodies for the treatment of carcinomas.                 
                These teachings are not applicable to the present invention, which recite[s]                  
                pharmaceutical compositions containing the immunogenic polypeptide                            
                GA733-2E.”  Page 7.  Appellants argue that “faced with the teaching of                        
                administration of antibodies (i.e., passive immunotherapy), one of skill in the art           
                would not have been motivated to prepare a pharmaceutical composition                         
                containing an immunogenic polypeptide (i.e., active immunotherapy).”  Page 8.                 
                      This argument is also not persuasive.  Claim 4 is directed to a                         
                “pharmaceutically acceptable composition” that comprises a “pharmaceutically                  
                effective amount” of truncated GA733-2 and a “pharmaceutically acceptable                     
                carrier.”  We agree with the examiner that this claim language reads on a                     
                composition containing the GA733-2 variant suggested by the cited references,                 
                and a carrier such as water, to be administered to an animal in order to raise                
                antibodies against GA733-2.                                                                   
                      Appellants seem to interpret the claim language to require a composition                
                that is administered to a patient for treatment (e.g., of cancer), but nothing in the         





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